首页> 外文期刊>Journal of Comparative Physiology, B. Biochemical, Systemic, and Environmental Physiology >Gene expression survey of mitochondrial uncoupling proteins (UCP1/UCP3) in gilthead sea bream (Sparus aurata L.)
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Gene expression survey of mitochondrial uncoupling proteins (UCP1/UCP3) in gilthead sea bream (Sparus aurata L.)

机译:金头鲷(Sparus aurata L.)线粒体解偶联蛋白(UCP1 / UCP3)的基因表达研究

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摘要

The aim of this work is to underline the biological significance of mitochondrial uncoupling proteins (UCPs) in ectothermic fish using the gilthead sea bream (Sparus aurata L.) as an experimental model. A contig of 1,990 bp in length was recognized as a UCP1 ortholog after initial searches in the gilthead sea bream AQUAFIRST database ( http://www.sigenae.org/aquafirst). Additional searches were performed in skeletal muscle by RT-PCR, and the amplified PCR product was recognized as UCP3 after sequence completion by 5'- and 3'RACE. UCP1 expression was mostly detected in liver, whereas UCP3 transcripts were only found in skeletal and cardiac muscle fibres (white skeletal muscle > red skeletal muscle > heart). Specific gene regulation of UCP1 (liver) and UCP3 (white skeletal muscle) was addressed in physiological models of age, seasonal growth and energy-metabolic unbalances. Both the increase in energy demand (stress confinement) and the reduction in energy supply during adaptive cold response in winter down-regulated UCP1 expression. Conversely, transcript levels of UCP3 were higher with age, seasonal fattening and dietary deficiencies in essential fatty acids leading to the increase in fatty acid flux towards the muscle. This close association between UCP1 and UCP3 with the oxidative and metabolic tissue status is perhaps directly related to the ancestral protein UCP function, and allows the use of UCPs as lipotoxicity markers in ectothermic fish.
机译:这项工作的目的是使用银头鲷(Sparus aurata L.)作为实验模型,来强调线粒体解偶联蛋白(UCPs)在外热鱼类中的生物学意义。在金头鲷AQUAFIRST数据库(http://www.sigenae.org/aquafirst)中进行初步搜索后,长度为1,990 bp的重叠群被识别为UCP1直系同源物。通过RT-PCR在骨骼肌中进行其他搜索,并在5'-和3'RACE序列完成后将扩增的PCR产物识别为UCP3。 UCP1表达主要在肝脏中检测到,而UCP3转录本仅在骨骼肌和心肌纤维中发现(白色骨骼肌>红色骨骼肌>心脏)。在年龄,季节性生长和能量代谢失衡的生理模型中,研究了UCP1(肝脏)和UCP3(白色骨骼肌)的特定基因调控。在冬季,UCP1表达下调时,在适应性冷反应期间能量需求的增加(应力限制)和能量供应的减少。相反,UCP3的转录水平随年龄,季节性肥胖和必需脂肪酸的饮食缺陷而升高,导致脂肪酸通向肌肉的流量增加。 UCP1和UCP3与氧化和代谢组织状态之间的这种紧密联系可能与祖先蛋白UCP功能直接相关,并允许将UCP用作吸热鱼类中的脂毒性标记。

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